United States · FDA National Drug Code directory
Diltiazem Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 24979-028_b08ee384-f82b-4f17-9e38-52ebc9187589
- Product NDC
- 24979-028
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Diltiazem hydrochloride
- Labeler
- Upsher-Smith Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181001
- Source listing expiry
- 20271231
Source-listed ingredients
- DILTIAZEM HYDROCHLORIDE — 240 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 24000 CAPSULE, EXTENDED RELEASE in 1 PACKAGE (24979-028-00) · 24979-028-00
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24979-028-02) · 24979-028-02
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24979-028-06) · 24979-028-06
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24979-028-07) · 24979-028-07
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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